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DOI: 10.1160/TH15-08-0637
Discontinuing early prophylaxis in severe haemophilia leads to deterioration of joint status despite low bleeding rates
Financial Support: The present study was funded by an unrestricted grant from Novo Nordisk. Dutch Trial Registry number 3098; UTN U1111–1121–7069.Publikationsverlauf
Received:
10. August 2015
Accepted after major revision:
22. Januar 2015
Publikationsdatum:
06. Dezember 2017 (online)
![](https://www.thieme-connect.de/media/10.1055-s-00035024/201605/lookinside/thumbnails/10.1160-th15-08-0637-1.jpg)
Summary
Prophylaxis is the recommended treatment for children with severe haemophilia A, but whether prophylaxis should be continued in adulthood is still under debate. Previous studies with limited follow-up have suggested that some patients may be able to stop prophylaxis in adulthood, while maintaining good joint health. This single-centre observational cohort study examined patients with severe haemophilia A born 1970–1988 without inhibitor development, and assessed the long-term consequences of discontinuing prophylaxis. Patient-initiated changes in prophylaxis, including all switches to on-demand treatment lasting a minimum of two consecutive weeks, were recorded from the time self-infusion began until the last evaluation. Sixty-six patients were evaluated at a median age of 32.4 years: 26 of patients had stopped prophylaxis for a median of 10 years, 15 had interrupted prophylaxis and 59 had continued prophylaxis. Annual joint bleeding rate (AJBR), Haemophilia Joint Health Score (HJHS-2.1; 0–124 points), radiological Pettersson score (0–78 points) and Haemophilia Activities List score (HAL; 100–0 points) were compared between patients who stopped and patients who continued prophylaxis. Although self-reported bleeding rates and functional limitations were similar in both groups (AJBR: 1.5 vs 1.2 and HAL: 84 vs 84 for those who stopped and continued prophylaxis, respectively), objective assessment of joint status showed increased arthropathy after 10 years of on-demand treatment in patients who stopped prophylaxis compared with those who continued (HJHS: 23 vs. 14 and Pettersson: 16 vs 5, respectively; P< 0.01). These results support continuation of long-term prophylaxis in adults and demonstrate the need for objective monitoring of joint status.
Trial registration: Dutch Trial Registry number 3098; UTN U1111–1121–7069.
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References
- 1 Van Creveld S. Prophylaxis of joint hemorrhages in haemophilia. Acta Haematol 1971; 45: 120-127.
- 2 Nilsson IM, Berntorp E, Lofqvist T. et al. Twenty-five years’ experience of prophylactic treatment in severe haemophilia A and B. J Intern Med 1992; 232: 25-32.
- 3 Srivastava A, Brewer AK, Mauser-Bunschoten EP. et al. Guidelines for the management of haemophilia. Haemophilia 2013; 19: e1-e47.
- 4 Van Dijk K, Fischer K, Van der Bom JG. et al. Can long-term prophylaxis for severe haemophilia be stopped in adulthood? Results from Denmark and the Netherlands. Br J Haematol 2005; 130: 107-112.
- 5 Richards M, Altisent C, Batorova A. et al. Should prophylaxis be used in adolescent and adult patients with severe haemophilia? An European survey of practice and outcome data. Haemophilia 2007; 13: 473-479.
- 6 Lindvall K, Colstrup L, Wollter IM. et al. Compliance with treatment and understanding of own disease in patients with severe and moderate haemophilia. Haemophilia 2006; 12: 47-51.
- 7 Fischer K, Van der Bom JG, Prejs R. et al. Discontinuation of prophylactic therapy in severe haemophilia: incidence and effects on outcome. Haemophilia 2001; 7: 544-550.
- 8 Du Treil S, Rice J, Leissinger CA. Quantifying adherence to treatment and its relationship to quality of life in a well-characterized haemophilia population. Haemophilia 2007; 13: 493-501.
- 9 De Moerloose P, Urbancik W, Van den Berg H. M.. et al. A survey of adherence to haemophilia therapy in six European countries: results and recommendations. Haemophilia 2008; 14: 931-938.
- 10 Collins PW, Blanchette VS, Fischer K. et al. Break-through bleeding in relation to predicted factor VIII levels in patients receiving prophylactic treatment for severe haemophilia A. J Thromb Haemost 2009; 7: 413-420.
- 11 Berntorp E, Astermark J, Bjorkman S. et al. Consensus perspectives on prophylactic therapy for haemophilia: summary statement. Haemophilia 2003; 9 (Suppl. 01) 1-4.
- 12 Richards M, Williams M, Chalmers E. et al. A United Kingdom Haemophilia Centre Doctors’ Organization guideline approved by the British Committee for Standards in Haematology: guideline on the use of prophylactic factor VIII concentrate in children and adults with severe haemophilia A. Br J Haematol 2010; 149: 498-507.
- 13 Makris M. Prophylaxis in haemophilia should be life-long. Blood Transfus 2012; 10: 165-168.
- 14 Manco-Johnson MJ, Sanders J, Ewing N. et al. Consequences of switching from prophylactic treatment to on-demand treatment in late teens and early adults with severe haemophilia A: the TEEN/TWEN study. Haemophilia 2013; 19: 727-735.
- 15 Manco-Johnson MJ, Abshire TC, Shapiro AD. et al. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe haemophilia. N Engl J Med 2007; 357: 535-544.
- 16 Nederlandse Vereniging van Hemofiliebehandelaars (NVHB). Richtlijn Diagnostiek en behandeling van hemofilie en aanverwante hemostasestoornissen. 2009; pp. 68-69.
- 17 Van Genderen FR, Westers P, Heijnen L. et al. Measuring patients’ perceptions on their functional abilities: validation of the Haemophilia Activities List. Haemophilia 2006; 12: 36-46.
- 18 Van Genderen FR, Van Meeteren NL, Van der Bom JG. et al. Functional consequences of haemophilia in adults: the development of the Haemophilia Activities List. Haemophilia 2004; 10: 565-571.
- 19 Blanchette VS, Key NS, Ljung LR. et al. Definitions in haemophilia: communication from the SSC of the ISTH. J Thromb Haemost 2014; 12: 1935-1939.
- 20 Hilliard P, Funk S, Zourikian N. et al. Haemophilia joint health score reliability study. Haemophilia 2006; 12: 518-525.
- 21 Creel GL, Light KE, Thigpen MT. Concurrent and construct validity of scores on the Timed Movement Battery. Phys Ther 2001; 81: 789-798.
- 22 Pettersson H, Ahlberg A, Nilsson IM. A radiologic classification of hemophilic arthropathy. Clin Orthop Relat Res 1980; 153-159.
- 23 De Moerloose P, Fischer K, Lambert T. et al. Recommendations for assessment, monitoring and follow-up of patients with haemophilia. Haemophilia 2012; 18: 319-325.
- 24 Fischer K, De Kleijn P. Using the Haemophilia Joint Health Score for assessment of teenagers and young adults: exploring reliability and validity. Haemophilia 2013; 19: 944-950.
- 25 Pettersson H, Nilsson IM, Hedner U. et al. Radiologic evaluation of prophylaxis in severe haemophilia. Acta Paediatr Scand 1981; 70: 565-570.
- 26 Fischer K, Steen Carlsson K, Petrini P. et al. Intermediate-dose versus high-dose prophylaxis for severe haemophilia: comparing outcome and costs since the 1970s. Blood 2013; 122: 1129-1136.
- 27 Fischer K, Ljung R, Platokouki H. et al. Prospective observational cohort studies for studying rare diseases: the European PedNet Haemophilia Registry. Haemophilia 2014; 20: e280-e286.
- 28 Schramm W, Royal S, Kroner B. et al. Clinical outcomes and resource utilization associated with haemophilia care in Europe. Haemophilia 2002; 8: 33-43.
- 29 Van Dijk K, Fischer K, Van der Bom JG. et al. Variability in clinical phenotype of severe haemophilia: the role of the first joint bleed. Haemophilia 2005; 11: 438-443.
- 30 Aledort LM, Haschmeyer RH, Pettersson H. A longitudinal study of orthopaedic outcomes for severe factor-VIII-deficient haemophiliacs. The Orthopaedic Outcome Study Group. J Intern Med 1994; 236: 391-399.
- 31 Molho P, Rolland N, Lebrun T. et al. Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France. Haemophilia 2000; 6: 23-32.
- 32 Rainsford SG, Hall A. A three-year study of adolescent boys suffering from haemophilia and allied disorders. Br J Haematol 1973; 24: 539-551.
- 33 Astermark J, Petrini P, Tengborn L. et al. Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized. Br J Haematol 1999; 105: 1109-1113.
- 34 Schwartz CE, Bode R, Repucci N. et al. The clinical significance of adaptation to changing health: a meta-analysis of response shift. Qual Life Res 2006; 15: 1533-1550.
- 35 Fischer K, Bom JG, Mauser-Bunschoten EP. et al. Effects of haemophilic arthropathy on health-related quality of life and socio-economic parameters. Haemophilia 2005; 11: 43-48.